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( Elizabeth Storck Kraemer Memorial Foundation and Department of Pathology, Jefferson Medical College and Hospital, Philadelphia, Pennsylvania)
The administration of 0.4 mg. of N,N'-(4-methyl-m-phenylene)-bis(aziridinecarboxamide)/100 gm body weight intraperitoneally 3 times weekly to 100 rats of the Sprague-Dawley strain bearing the transplantable Walker mammary carcinoma 256 produced complete regression of tumor in 68 animals and a favorable response in 31 others, giving a total salutary effect of 99 per cent. Of 85 animals treated with 0.25 cc. of physiologic saline/100 gm body weight intraperitoneally daily, four showed complete regression of tumor, and none showed a favorable response, giving a total salutary effect of 4.7 per cent. Of 66 animals treated with 0.4 mg triethylene melamine/100 gm body weight by stomach tube once weekly, 41 disclosed complete regression of tumor, and nine disclosed a favorable response, giving a total salutary effect of 75.8 per cent. Under the conditions of this experiment it is concluded that N,N'-(4-methyl-m-phenylene)-bis(aziridinecarboxamide) is a better tumor-inhibitor than is triethylene melamine. Administered by stomach tube, however, the total necessary dose of N,N'-(4-methyl-m-phenylene)-bis(aziridinecarboxamide) is 25 times that of triethylene melamine, and its effectiveness is greatly reduced.
Received 5/16/55.
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